# FDA Inspection 1264168 - Mitchell Miller, MD - February 21, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/mitchell-miller-md/d85239e2-ecb1-400f-aa74-378298a57e93
Source feed: FDA_Inspections

> FDA Inspection 1264168 for Mitchell Miller, MD on February 21, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1264168
- Company Name: Mitchell Miller, MD
- Inspection Date: 2025-02-21
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1264168 - 2025-02-21](https://www.globalkeysolutions.net/records/fda_inspections/mitchell-miller-md/d9d3f08f-fa8c-4e98-bc03-bdc99d1115d0)
- [FDA Inspection 1032572 - 2017-11-06](https://www.globalkeysolutions.net/records/fda_inspections/mitchell-miller-md/49627a88-e788-408f-8dfd-5d7bd2dacc10)

Company: https://www.globalkeysolutions.net/companies/mitchell-miller-md/420ba81b-58c4-4d6e-8e36-6e8d683d7de6

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7